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Via Catania 30
65019 Pianella (PE)

+39 071 9257675

info@seamautomation.com

    Isolator Systems

    SEAM

    pharmaceutical sectorOptimize production processes

    In pharmaceutical processes, production under isolator systems is essential to ensure maximum protection against contamination and to meet strict quality and safety standards. Our software for isolator machines is designed to optimize production processes within sterile environments, managing each stage of dosing, mixing, and packaging with precision while ensuring full compliance with regulations such as GMP (Good Manufacturing Practices) and FDA standards.

    pharmaceutical sectorWhat We Offer:

    Precise Control of Isolator Processes

    Management of automated machines and systems operating in sterile environments, such as negative-pressure isolators, ensuring accurate dosing and processing

    Integration with Isolators and Existing Systems

    Our software easily interfaces with dosing, filling, sterilization, and other machines, optimizing the entire workflow

    Real-time Monitoring of Environmental Conditions

    Managing parameters such as temperature, humidity, and pressure to maintain sterile conditions throughout production

    Compliance with Pharmaceutical Regulations

    The software is designed to meet GMP, FDA, and other safety and quality regulations required in sterile and protected environments

    Advanced Security and Traceability

    Automatic generation of detailed reports to track every stage of the process, ensuring complete safety and compliance during audits and inspections

    Intuitive User Interfaces

    Simple and clear control panels to facilitate operation monitoring without compromising security

    Complete Process Automation

    Reducing human errors and increasing operational efficiency through automation and continuous system monitoring

    pharmaceutical sectorKey Benefits:

    Strict control of sterile conditions to ensure product quality and safety

    Process automation that reduces the risk of errors and optimizes productivity

    Full traceability and compliance with pharmaceutical industry regulations

    Enhanced safety and protection against contamination in critical environments